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Gene

SLC30A5

solute carrier family 30 member 5

Summary

Cytogenetic location
5q13.1-q13.2
Coordinates
Chromosome 5: 69,094,014–69,131,069 (GRCh38)
Exons
16 exons across 37.1 kb
Protein
765 amino acids
Also known as
ZTL1, ZnT-5, FLJ12496, FLJ12756, ZNT5, MGC5499, ZNTL1
MANE Select transcript
ENST00000396591.8NM_022902.5
Locus type
gene with protein product

Reference genomeGRCh38

Positions on gene and variant pages follow this choice, in this browser.

Curated reports relevant to this gene

No Genome Test report reads SLC30A5 yet. The test sequences your whole genome, so your data includes it all the same.

How SLC30A5 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 5, with a bracket where SLC30A5 sits. SLC30A5 and 11 genes near it on chromosome 5, from 68,612,542 to 69,612,541.Chromosome 55q13.1-q13.2p15.33p15.32p15.31p15.2p15.1p14.3p14.2p14.1p13.3p13.2p13.1p12p11q11.1q11.2q12.1q12.2q12.3q13.1q13.2q13.3q14.1q14.2q14.3q15q21.1q21.2q21.3q22.1q22.2q22.3q23.1q23.2q23.3q31.1q31.2q31.3q32q33.1q33.2q33.3q34q35.1q35.2q35.368.8 Mb69 Mb69.2 Mb69.4 Mb69.6 MbSLC30A5: 69,094,014–69,131,069, forward strandSLC30A5CCNB1: 69,167,004–69,178,389, forward strandCCNB1CENPH: 69,189,537–69,210,357, forward strandCENPHKGD4: 69,217,712–69,231,410, forward strandKGD4CDK7: 69,234,550–69,277,495, forward strandCDK7CCDC125: 69,279,859–69,332,828, reverse strandCCDC125AK6: 69,333,643–69,370,026, reverse strandAK6TAF9: 69,362,026–69,370,026, reverse strandTAF9RAD17: 69,369,293–69,414,806, forward strandRAD17MARVELD2: 69,415,065–69,444,330, forward strandMARVELD2OCLN: 69,492,184–69,558,114, forward strandOCLNGTF2H2C: 69,558,392–69,595,221, forward strandGTF2H2CDiagram of SLC30A5: 16 exons on the forward strand of chromosome 5Exon 9: 1 known disease-causing siteExon 14: 1 known disease-causing siteExon 1: 69,094,014–69,094,338, 325 basesExon 2: 69,100,807–69,100,929, 123 basesExon 3: 69,103,062–69,103,128, 67 basesExon 4: 69,104,631–69,104,716, 86 basesExon 5: 69,108,349–69,108,436, 88 basesExon 6: 69,113,140–69,113,227, 88 basesExon 7: 69,114,420–69,114,496, 77 basesExon 8: 69,115,237–69,115,407, 171 basesExon 9: 69,115,926–69,116,214, 289 basesExon 10: 69,116,394–69,116,602, 209 basesExon 11: 69,117,239–69,117,396, 158 basesExon 12: 69,118,499–69,118,628, 130 basesExon 13: 69,121,694–69,121,895, 202 basesExon 14: 69,123,199–69,123,425, 227 basesExon 15: 69,128,004–69,128,132, 129 basesExon 16: 69,129,447–69,131,069, 1,623 bases12468101214165′3′

Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.

Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).

Nearby genes from Ensembl release 116, on GRCh38.

Exons make up 4 kb of the gene's 37.1 kb; 2,298 of those bases code for the protein.

How a genome test reads SLC30A5

2

positions in SLC30A5 where ClinVar classes a change as pathogenic or likely pathogenic

None of them falls in a region short reads find hard.

A whole genome covers all 37.1 kb of SLC30A5, introns included, not only the 4 kb of exons.

Where this comes from

  • HGNC: the gene's symbol, name, other symbols and location.
  • MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
  • ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
  • Data release 2026.10.16-c6eea6bf.

Cite this page

APA

Dante Labs. (n.d.). SLC30A5 gene: solute carrier family 30 member 5. Retrieved 16 October 2026, from https://dantelabs.com/genes/slc30a5

Vancouver

Dante Labs. SLC30A5 gene: solute carrier family 30 member 5 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/slc30a5

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